ZipRecruiter

Log In

1

Temporary Quality Iso 9001 Jobs in Riverside, CA

Atln

Supplier Quality Engineer / QMS Auditor

Tustin, CA · On-site

$100 - $125/hr

Conduct internal audits and supplier audits to ensure compliance with QMS standards (e.g., ISO 9001, AS9100). * Evaluate suppliers' Quality Management Systems (QMS) to verify alignment with safety ...

Balda C Brewer

Quality Manager (ISO 13485)

Ontario, CA · On-site

$140K - $180K/yr

As a quality manager you will ensure that the manufacturing site meets and applies the Global Quality Policies and Guidelines relating to, ISO 9001 & 13485 standards, FDA 21 CFR 820 regulations ...

ADURA LLC

Quality Control Manager

Corona, CA · On-site

$100K - $120K/yr

Key Responsibilities: • Lead quality assurance processes for incoming inspection, in-process control, and final QC. • Maintain and enhance the quality management system (QMS) for ISO 9001 ...

Clariant SE

Quality Lead

Colton, CA · On-site

$100 - $125/hr

Lean 6 Sigma (preferred), 5S, ISO 9001 & QA Experience * Proficient with Microsoft Office Suite * SAP preferred What's in it for you? * Paid Holidays * PTO time with a carry-over benefit * Tuition ...

CYNET SYSTEMS

Inspector II

Rancho Cucamonga, CA · On-site

$26 - $31/hr

ISO 9001-15. * Quality Inspection. * Internal Audits. Qualification And Education: * High School Diploma or GED. Benefits Our Benefits Include: * Medical, Dental, and Vision Insurance * 401(k) ...

Adecco

Quality Inspector

Rancho Cucamonga, CA · On-site

$30.82/hr

Maintain knowledge of quality standards including AS9100D, AS9120B, and ISO 9001:2015, adhere to internal work instructions, and assist with conducting internal quality audits. Candidates for Quality ...

next page

Showing results 1-20

All JobsQuality Iso 9001 JobsTemporary Quality Iso 9001 JobsTemporary Quality Iso 9001 Jobs in Riverside, CA

Temporary Quality Iso 9001 information

See Riverside, CA salary details

$12

$21

$33

How much do temporary quality iso 9001 jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for temporary quality iso 9001 in Riverside, CA is $21.27, according to ZipRecruiter salary data. Most workers in this role earn between $16.78 and $24.09 per hour, depending on experience, location, and employer.

What does a temporary Quality ISO 9001 professional do?

A Temporary Quality ISO 9001 professional is responsible for ensuring that an organization's processes and products meet the standards outlined in the ISO 9001 quality management system, often on a contract or short-term basis. Their duties typically include conducting audits, reviewing documentation, identifying areas for improvement, and helping teams comply with ISO 9001 requirements. They may also assist in preparing for external certification audits and training staff on quality standards. This role is crucial for maintaining consistent product quality and supporting continuous improvement within the company.

What are the key skills and qualifications needed to thrive as a temporary Quality ISO 9001 specialist?

To thrive as a Temporary Quality ISO 9001 Specialist, you need a strong understanding of quality management systems, auditing processes, and ISO 9001 standards, often backed by relevant experience or certification. Familiarity with quality management software, document control systems, and auditing tools is typically required. Strong attention to detail, problem-solving abilities, and effective communication skills help in identifying non-conformities and facilitating improvements. These skills ensure compliance with ISO standards, support continuous improvement, and help organizations maintain high-quality processes.

What are the common challenges faced by someone working in a temporary Quality ISO 9001 role?

In a temporary Quality ISO 9001 role, professionals often face the challenge of quickly adapting to an organization’s existing processes and quality management systems. They must rapidly familiarize themselves with the company's documentation, audit schedules, and compliance requirements while ensuring that standards are consistently met. Additionally, temporary staff may need to build rapport with permanent team members and effectively communicate quality objectives, often with limited time to integrate fully. Balancing immediate project responsibilities with ongoing quality improvement initiatives is also a key aspect of the role.

What is the difference between Temporary Quality Iso 9001 vs Temporary Quality Auditor?

AspectTemporary Quality Iso 9001Temporary Quality Auditor
CertificationsISO 9001 Lead Auditor, Quality Management System (QMS) certificationsISO 9001 Lead Auditor, QMS certifications
Work EnvironmentImplementing and maintaining ISO 9001 standards within organizationsAuditing and assessing compliance of quality systems
Employer & Industry UsageManufacturing, healthcare, service industries focusing on quality managementManufacturing, certification bodies, consulting firms

Temporary Quality Iso 9001 professionals focus on implementing and maintaining ISO 9001 standards, ensuring organizations meet quality management requirements. Temporary Quality Auditors primarily evaluate and verify compliance through audits. While both roles require ISO 9001 certifications, their responsibilities differ: one implements standards, the other assesses adherence.

What are the most commonly searched types of Quality Iso 9001 jobs in Riverside, CA?

The most popular types of Quality Iso 9001 jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Temporary Quality Iso 9001 jobs?

Cities near Riverside, CA with the most Temporary Quality Iso 9001 job openings:

Temporary Quality Iso 9001 jobs near you
Infographic showing various Temporary Quality Iso 9001 job openings in Riverside, CA as of August 2026, with employment types broken down into 92% Full Time, 4% Temporary, 2% Contract, and 2% Nights. Highlights an 98% In-person, and 2% Remote job distribution, with an average salary of $44,252 per year, or $21.3 per hour.

Quality Engineer (ISO 9001, 13485)

Balda C Brewer

Ontario, CA • On-site

$90K - $130K/yr

Full-time

Re-posted 12 days ago

Key responsibilities

  • Support the development and manufacturing of medical devices in conformance with applicable ISO 13485 requirements.

  • Collaborate with Program Managers, Process Engineers, and Validation Engineers to execute process and equipment qualifications.

  • Plan and perform regular audits of the quality system and drive system improvements through internal audits and quality event management.

Job description

Quality Engineer supports all aspects of the Quality Management System, Product Realization and Manufacturing Process Controls. Working with cross functional partners, defines and generates quality control plans, production process controls and procedures. Leads and supports validations including statistical analysis. Engages with customers to address quality issues and define acceptance criteria/attributes.

Essential Job Functions and Responsibilities:

  • Support the development and manufacturing of medical devices in conformance with applicable ISO 13485 requirements. Responsible for quality planning of all new development programs and design transfers to production.
  • Ensure policies and procedures comply with regulations and external standards, including software regulations, risk management, and change control.
  • Interact and form constructive working relationships with all levels of leadership within Quality, Procurement, Marketing, Engineering, and Operations.
  • Collaborate with Program Managers, Process Engineers, and/or Validation Engineers to execute process and equipment qualifications.
  • Problem Resolution: identification, data collection and trend analysis, reporting, and initiation of corrective and/or preventive action as well as reporting out of Key Metrics.
  • Identify opportunities and implement solutions to drive continuous improvement in performance metrics.
  • Investigate customer complaints, corrective actions and trending to drive improvements. * Plan and perform regular audits of quality system and drive system improvements through the Internal Audit and Quality Event Management (CAPA, NCR, Complaint etc.)
  • Monitoring and improvement of SPC systems, sampling plans and statistical methods. * Back-up and or perform to Head of Site Quality/Supervisor Representative, as assigned.
  • Plan, prepare, and execute Internal Audits, as assigned.
  • Participate in Material Review Board and/or Change Control Board as QA representative.
  • Utilize tools, gauges and other inspection equipment to obtain product specification data * Expert in utilizing hand measurement tools (Caliper, Micrometer, Ruler, Gage Blocks, height gage, etc.).
  • High Proficiency with PCDMIS inspection software utilizing CMM’s: Brown, Sharpe, Hexagon, Smart scope.
  • Expert with utilizing ANSI Sampling Plans, IQMS, Minitab, Excel and Microsoft Word
  • High Proficiency in material analysis (i.e. FTIR, Melt Flow Testing, etc.)
  • Ability to read and decipher blueprints * Proficient in metrology and calibration.
  • Working knowledge of statistical methods for manufacturing.
  • Proficient in Geometric Dimensioning and Tolerancing (ANSI Y-14.5)

Requirements:

  • Minimum Education: five (5) years’ experience in a similar field. Working knowledge in problem solving methodologies. Excellent oral and written communication skills.
  • Minimum Experience: At least two (2) year experience in a supervision and/or management role. Demonstrated experience to lead teams and projects. Good organizational skills. Previous experience in plastic injection molding related environment.
  • Demonstrated experience to lead teams and projects. Good organizational skills. Previous experience in plastic injection molding related environment.
  • Working in a medical device or other FDA regulated industry. Comprehensive understanding of ISO 9001, ISO 13485, JPAL MHLW Ordinance 169, and/or FDA QSR regulatory requirements. Computer literate with working knowledge of MS Word, Excel, and Access.
  • Desired candidate will have prior work history in MSA, SPC, Mini-tab, Infinity, sterilization, & clean room environment. *Knowledge, Skills, and Abilities
  • A working knowledge of FDA cGMP, ISO13485 requirements
  • A working knowledge of medical device manufacturing quality systems.
  • Working knowledge of Statistical Methods used in manufacturing. * PC-DMIS knowledge a plus.

Education and/or Experience:

  • 3-7 Years in Quality Engineering in manufacturing and/or quality assurance.
  • Training in applicable ISO 9001, ISO 13485.
  • Experience using Minitab.
  • Proficient in metrology and calibration standards.
  • Proficient in Quality Audit concepts.
  • FDA quality standards experience a plus.
  • Certifications such as ASQ CQE, CQA, CQM
  • Warehouse areas (limited)
  • Will be required to perform other duties as requested, directed or assigned.

Apply